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1.
X-ray diffraction and oxygen isotopic analyses of outcrop and subsurface samples of siliceous rocks were used to reconstruct thermal and diagenetic histories of the Miocene Monterey Shale near Santa Maria, California. Within many stratigraphic sections soft, porous diatomaceous rocks change gradationally to underlying hard and brittle chert, porcellanite, and siliceous shale; the accompanying silica mineral zones are, in descending stratigraphic order: (1) biogenic silica (opal-A), (2) cristobalitic silica (opal-CT), and (3) microcrystalline quartz. Boundaries between silica mineral zones and stratigraphic horizons are often discordant. Within the opal-CT zone, the d(101)-spacing of opal-CT decreases in a smooth non-linear fashion from about 4 10 Å to 4-04 Å. In the Santa Maria Valley and Bradley oil field areas the thicknesses of the opal-CT zones are greater and the present thermal gradients less than in the adjacent Orcutt oil field. Thin opal-CT zones at shallow maximum burial depths apparently correlate with higher thermal gradients. Using present thermal gradients and reconstructed maximum burial depths from well data in the Santa Maria region, the ranges in temperatures for the top and base of the opal-CT zone are 38–54 °C and 55–110 °C, respectively. The temperature difference between these two boundaries ranges from 17 to 60 °C. In comparison, temperature ranges for these two boundaries computed from oxygen isotopic compositions of opal-CT and quartz, extrapolated experimental quartz-water fractionations, and assuming δO18= 0%o for the isotopic composition of the equilibrating fluid are 18–56 °C and 31–80 °C for the top and base of the opal-CT zone, respectively. The temperature difference between these boundaries is 11–36 °C using this method. Thermal gradients and sedimentation rates strongly influence rates of silica transformations. Reconstructed thermal and diagenetic histories of siliceous rocks of the Monterey Shale at four well sites in the Santa Maria region demonstrate that most silica conversions probably occurred during the last 3–4 Myr in response to accelerated rates of sedimentation (and therefore burial heating) during the Pliocene.  相似文献   

2.
Marine diatomaceous siliceous sediments in Neogene sections of northern Japan contrast with the Monterey Shale of California in containing many intercalations of acidic volcaniclastic sediments. Diagenesis of these sediments from deep boreholes and surface sections was investigated. Three diagenetic zones—biogenic opal, opal-CT and quartz zones—are recognized in siliceous sediments, corresponding roughly to amorphous silica, low cristobalite and quartz zones in acidic vitric volcaniclastic sediments. Opal-CT consists almost exclusively of silica and water, while low cristobalite contains appreciable amounts of A1, Ca, Na and K. In subsurface sections, values of d(101) spacing of opal-CT decrease progressively with increasing burial depth. The progressive ordering is not associated with additional silica cementation. In surface sections, the behaviour of d(101) spacing is complicated owing to the modification of the progressive ordering developed during burial diagenesis by later silica cementation during uplift. The cementing opal-CT is probably precipitated from percolating groundwater which dissolves siliceous skeletons in porous diatomaceous mudstones overlying the opal-CT porcellanite. Opaline cherts that form during burial diagenesis are designated as early opaline chert, while those which form during uplift are later opaline chert. The later opaline chert contains two groups of opal-CT; one is progressively ordered opal-CT and the other is additionally cemented opal-CT with higher d(101) spacing than that in the host porcellanite. In diatomaceous siliceous sediments, early opaline chert is scarce. Most, if not all, opaline cherts in surface sections are of later origin.  相似文献   

3.
Diatom ooze and diatomaceous mudstone overlie terrigenous mudstone beds at Leg 19 Deep Sea Drilling Project sites. The diatomaceous units are 300-725 m thick but most commonly are about 600 m. Diagenesis of diatom frustules follows a predictable series of physical and chemical changes that are related primarily to temperature (depth of burial and local geothermal gradient). During the first 300-400 m of burial frustules are fragmented and undergo mild dissolution. By 600 m dissolution of opal-A (biogenic silica) is widespread. Silica reprecipitates abundantly as inorganic opal-A between 600 and 700 m sub-bottom depth. Inorganic opal-A is rapidly transformed by crystal growth to opal-CT. The result is formation of silica cemented mudstone and porcelanite beds. A regional acoustic reflector (called the bottom-simulating reflector, or BSR) occurs near 600 m depth in the sections. This acoustic event marks the upper surface where silicification (cementation) is active. In Bering Sea deposits, opal-A is transformed to opal-CT at temperatures between 35° and 50°C. This temperature range corresponds to a sub-bottom depth of about 600 m and is the area where silicification is most active. Thus, the BSR represents an isothermal surface; the temperature it records is that required to transform opal-A to opal-CT. Deposition of at least 500 m of diatomaceous sediment was required before the temperature at the base of the diatomaceous section was appropriate (35°-50°C) for silica diagenesis to occur. Accordingly, silica diagenesis did not begin until Pleistocene time. Once silicification began, in response to sediment accumulation during the Quaternary, the diagenetic front (the BSR) moved upsection in pace with the upward migrating thermal boundary. X-ray diffractograms and SEM photographs show three silica phases, biogenic opal-A, inorganic opal-A’, and opal-CT. These have crystallite sizes of 11-16 A, 20-27 A, and 40-81 A, respectively, normal to 101. The d(101) reflection of opal-CT decreases with depth of burial at DSDP Site 192. This occurs by solid-state ordering and requires at least 700 m of burial. Most clinoptilolite in Leg 19 cores forms from the diagenesis of siliceous debris rather than from the alteration of volcanic debris as is commonly reported.  相似文献   

4.
A Tertiary non-marine stratigraphic sequence composed of carbonates(limestone),siliceous carbonates,coaly layers overlain by pyroclastic rocks and lavas,outcrops in the Gavatha area of northwestern Lesvos Island.Pure earbonates eonsist almost completely of calcite,the siliceous carbonate sediments of quartz,opal-CT and calcite,the shales of quartz,opal CT, K-feldspar,smecite-illite and ealcite,and the coaly layers of organic matter,quartz,opal-CT,feldspars and pyrite,Geochemical data indicate that smectite-illite,feldspars and associated elements(La,Zr,Y,Ba,Ce)are the products of alteration of volcanic rocks in a subtropical area A combination of sources in suggested for the formation of silica polymorphs:(a) biogenic or non-biogenic silica(opal-A) that was originally present in the form of diatiom frustules of in the form of inorganically prccipitated silica;(b)transformation o opall-A to opal-CT and quartz opal-C from alteration of volcanic glass of intercalated tuffites and overlying volcanics;and(c)opal-CT deposited primarily from hydrothermal solutions.  相似文献   

5.
The Coniacian Arnager Limestone Formation is exposed on the Danish island of Bornholm in the Baltic Sea. It is composed of mound-bedded siliceous chalk, and X-ray diffraction and scanning electron microscopy indicate a content of 30–70% insoluble minerals, including authigenic opal-CT, quartz, clinoptilolite, feldspars, calcite, dolomite, and barite. Opal-CT and clinoptilolite are the most common and constitute 16–53% and 2–9%, respectively. The content of insoluble minerals varies laterally both within the mounds and in planar beds, and the opal-CT content varies by up to 10% vertically. The mounds consist of two microfacies, spiculitic wackestone and bioturbated spiculitic wackestone, containing 10–22% and 7–12% moulds after spicules, respectively.Subsequent to deposition and shallow burial, dissolution of siliceous sponge spicules increased the silica activity of the pore water and initiated precipitation of opal-CT. The opal-CT formed at temperatures around 17 °C, the precipitation lowered the silica activity and the Si/Al ratio of the pore water, resulting in precipitation of clinoptilolite, feldspar and smectite. Calcite formed synchronously with the latest clinoptilolite. Minor amounts of quartz precipitated in pore water with low silica activity during maximum burial, probably to depths of 200–250 m. The dissolution of sponge spicules and decomposition of the sponge tissue also resulted in the release of Ba2+, Sr2+, Mg2+, Ca2+ and CO32?, facilitating precipitation of barite and dolomite. Precipitation of especially opal-CT reduced the porosity to an average of 40% and cemented the limestone. The study highlights the diagenetic pathways of bio-siliceous chalk and the effects on preservation of porosity and permeability.  相似文献   

6.
Some of the Lower Pleistocene bentonites of Milos and Kimolos islands, Greece, are valued for their white colour and physicochemical properties. They contain opal-CT and, sometimes, zeolite along with smectite, and have been derived from the alteration of rhyolitic volcanic rocks. The Miloan white bentonites contain Tatatilla-type montmorillonite and beidellite. The Kimolian ones have Chambers-type montmorillonite. The alteration process involved removal of alkalis and uptake of Mg, probably from sea water. Si is either redistributed or partially removed. The Kimolian white bentonites have higher brightnesses, L* and whiteness index values, and lower yellowness index and ΔE*ab values compared with the Miloan ones. The variations in white colour are inversely related to the abundance of Fe oxides and anatase, the occurrence of Fe in the smectite structure and its oxidation state. The presence of silica minerals is not an important factor affecting colour, but is undesirable since it imparts high abrasiveness in commercial products. The formation of white bentonites of high quality requires the removal of alkalis and silica during alteration of acid volcanics in order to avoid crystallization of zeolites and opal-CT. Fe needs to be incorporated into the smectite structure. Such conditions are rarely attained. Received: 25 September 1996 / Accepted: 17 January 1997  相似文献   

7.
The present study reports the results of research on volcaniclastic products from Logudoro (northern Sardinia), a reconstructed stratigraphic succession some hundreds of meters thick, comprising two different ignimbritic units separated by an epiclastic layer (generally ˜10 m thick). Clinoptilolite is the most widely distributed authigenic phase in epiclastite and unwelded units, always associated with opal-CT and sometimes with smectite. An adularia-like feldspar, cristobalite and epigenetic quartz are typical phases of welded units. Within the zeolitized units (unwelded ignimbrite and epiclastic units) clinoptilolite and opal-CT constitute the cement deriving from the transformation of the precursor rhyolitic glass, in agreement with a single zeolitization process that developed after the deposition of the entire succession. Silica increases in zeolitized rocks with respect to the precursor material, leading to hypothesize that the secondary mineralization process was favored by mineralized hydrothermal fluids preferentially circulating through the fault system of the area. Quartz veins in welded subunit and K-feldspar (adularia-like) preferentially located near the faults are in agreement with this hypothesis. The interaction of these fluids with the glassy fraction favored its dissolution and the consequent crystallization of clinoptilolite. Furthermore, the pH increase and the silica supersaturation enhanced the contemporary or subsequent precipitation of opal-CT. Received: 5 June 2000 / Accepted: 14 August 2000  相似文献   

8.
In low grade metabasites the amphibole components tremolite, glaucophane, edenite and tschermakite have their activities controlled by interactions with the excess components albite, clinozoisite, chlorite, quartz and H2O vapor. Three types of reaction are involved, (i) Those in which only components of condensed phases take part: isopleths of equilibrium constant are straight lines in the P-T plane. (ii) Dehydration reactions in which entropy change due to change in Al coordination is of the same sign as that due to dehydration: isopleths of constant K are positive at low pressure and negative at high pressure. (iii) Dehydration reactions in which entropy change due to Al coordination change is opposite in sign to that of dehydration: isopleths of constant K loop in the P-T plane with positive slopes at low and at high pressure. Zonation in naturally occurring amphiboles records the evolution of metamorphic conditions in particular rocks. In an example from the eastern Alps (Austria) early conditions calculated as 15 kb, 200 ° C evolve upgrade to 6 kb, 525 ° C implying concurrent heating and erosion. The record of evolving conditions may span some 30 Ma of geological history.  相似文献   

9.
Experimental investigations on model single pile anchor and pile group anchors of configuration 2 × 2 subjected to uplift loads were conducted on dry Ennore sand, obtained from Madras, India. The embedment length to shaft width ratios, L/d = 20 and L/d = 30, and enlarged base width to shaft width ratios, B/d = 1,2,3, center to center spacing of pile anchors in the groups, 3d, 4d, 6d and 8d were used. The load displacement response, ultimate resistance and variation of group efficiency with L/d, B/d and spacing have been studied quantitatively and qualitatively. For short pile group anchors (L/d = 20), the isolation spacing appears to be at a spacing of about 4d to 6d and 8d for B/d = 1 and B/d = 2 and 3, respectively. For long pile group anchors (L/d = 30), the isolation spacing appears to be at a spacing of about 4d, 6d and 8d for B/d = 1, 2 and 3, respectively. The analytical model of limit equilibrium method has been proposed to predict the net uplift capacity of pile group anchors. The predicted results compare reasonably well with the experimental results.  相似文献   

10.
A field study was conducted on two mountain streams in the Cascade Mountains of Washington State on the morphological characterization of cluster microforms. Morphological characterization of clusters is presented in terms of: (i) cluster shape; (ii) cluster geometric properties; and (iii) the spatial arrangement of clusters in the horizontal plane. Clusters were differentiated from other microtopography features such as reticulate structures and transverse ribs, and identified clusters were categorized by shape as being of pebble, line, comet, heap or ring type. The complex spatial arrangement of clusters at the sites was characterized by using a two‐dimensional correlation function, which allowed for measurement of the average cluster‐spacing properties. For the rivers examined, pebble‐shaped clusters were the most frequently observed cluster shape. Cluster geometric properties were found to be controlled by particles of the largest size fraction in the bed and the projected frontal width of the cluster – with cluster length being linearly related to cluster width for cluster width‐to‐height ratios <3·5. Results of the cluster‐spacing analysis suggest that cluster spacing increases with cluster size and decreases with local slope. Application of this principle to the available spacing data shows that cluster spacing λ scales with the ratio of S/d0 such that λS/d0 = constant, where S is the local slope and d0 the diameter of the largest particle in the cluster.  相似文献   

11.
Mineralogical and textural changes accompanying ageing of silica sinter   总被引：3，自引：0，他引：3  
Twenty nine samples of silica sinter, ranging in age from modern to Miocene, record temporal changes in both mineralogy and texture. When first deposited, sinters consist largely of noncrystalline spheres (<1–8 μm diameter) of opal-A exhibiting varying degrees of close-packing. Particle densities range from 1.5 to 2.1 g cm−3, total water 4–10 wt%, and porosities 35–60%. Changes over ∼10,000 years following deposition are slight although the spheres may be invested by an additional film of secondary silica. For the next 10,000 to ∼50,000 years, the silica incrementally crystallises to become poorly crystalline opal-CT and/or opal-C; spherical particles of thin-bladed crystals (lepispheres) replace opal-A particles and coalesce in microbotryoidal aggregates (∼10–30 μm diameter). Amygdaloidal fibrous clusters occur with lepispheres. As silica lattice ordering becomes enhanced, total water content drops to <7 wt%, particle density increases to ∼2.3 g cm−3, and porosity reduces to <30%. The change from opal-A to opal-C takes place over a briefer periods (∼50 years) in silica sinters that contain other materials (e.g. calcite, sulfur, alunite, plant remains). Sinters older than ∼50,000 years have recrystallised to microcrystalline quartz. With the onset of quartz crystallisation at ∼20,000 years, total water is <0.2 wt%, particle density approximates quartz (2.65 g cm−3), and porosity is <4%. The progressive changes in silica species and texture yield ageing profiles for sinters that may serve as guides to the paleohydrology of geothermal systems and/or epithermal ore deposits in areas where surface thermal activity has declined or ceased. Received: 18 November 1998 / Accepted: 6 July 1999  相似文献   

12.
A simulated annealing technique was used to search for global and local minimum energy structures of a potential energy model for silica. The model is based on ab initio SCF MO calculations on the disilicic acid molecule, H6Si2O7. Starting with 4 SiO2 units, with the atoms randomly distributed in the unit cell, 23 distinct silica tetrahedral framework structures were found, with a variety of space group symmetries and cell dimensions. Despite the assumption of P 1 space group symmetry for the starting structure, only 7 of the local minimum energy structures were found to possess triclinic symmetry with the remainder exhibiting symmetries ranging from P c to to within 0.001 Å. Although the interaction potential for the disilicic acid molecule has a single minimum energy SiO bond length and SiOSi angle, the local minimum energy structures exhibit angles that range between 105° and 180° and bond lengths that range between 1.55 and 1.68 Å. The correlation observed for coesite and the other silica polymorphs between SiO bond length and fs(O) is reproduced. The generated structures show a wide variety of coordination sequences, ring sizes and framework densities, the later ranging from 19.8 to 35.5 Si/1000 Å3. The energies of these structures correlate with their framework densities, particularly for higher energy structures.  相似文献   

13.
 We have determined the quenched cation ordering states of five orthopyroxene crystals collected from the marginal border group and the lower zone a and b of the Skaergaard intrusion, and modeled these data to retrieve their closure temperatures (T c) of Fe–Mg ordering and cooling rates. According to existing thermal models for the Skaergaard pluton, conductive cooling dominated the high and low temperature regimes, which were separated by an intermediate temperature regime in which the cooling was controlled primarily by convective fluid circulation. The cooling rates retrieved from the quenched cation ordering states of the orthopyroxene crystals strictly apply to temperatures around the closure temperatures of the ordering states, ∼340–400° C, which fall at the transition from convective to the lower temperature conductive cooling. The cooling rates obtained from the cation ordering states of orthopyroxene vary from ∼1 to 270 K/ka. These results agree well with a thermal model calculated using an assumed average permeability of 10-12 cm2 for the pluton, but not completely with a model calculated on the basis of an average permeability of 10-13 cm2, although both values produced shifts of δ18O that are comparable to those observed in the pluton. Received: 27 February 1995/Accepted: 20 July 1995  相似文献   

14.
Molecular dynamics (MD) computer simulations of liquid water held in one-dimensional nano-confinement by two parallel, electrostatically neutral but hydrophilic surfaces of brucite, Mg(OH)2, provide greatly increased, atomistically detailed understanding of surface-related effects on the spatial variation in the structural ordering, hydrogen bond (H-bond) organization, and local density of H2O molecules at this important model hydroxide surface. NVT-ensemble MD simulations (i.e., at constant number of atoms, volume and temperature) were performed for a series of model systems consisting of 3 to 30 Å-thick water layers (containing 35 to 360 H2O molecules) confined between two 19 Å-thick brucite substrate layers. The results show that the hydrophilic substrate significantly influences the near-surface water structure, with both H-bond donation to the surface oxygen atoms and H-bond acceptance from the surface hydrogen atoms in the first surface layer of H2O molecules playing key roles. Profiles of oxygen and hydrogen atomic density and H2O dipole orientation show significant deviation from the corresponding structural properties of bulk water to distances as large as 15 Å (∼5 molecular water layers) from the surface, with the local structural environment varying significantly with the distance from the surface. The water molecules in the first layer at about 2.45 Å from the surface have a two-dimensional hexagonal arrangement parallel to brucite layers, reflecting the brucite surface structure, have total nearest neighbor coordinations of 5 or 6, and are significantly limited in their position and orientation. The greatest degree of the tetrahedral (ice-like) ordering occurs at about 4 Å from the surface. The translational and orientational ordering of H2O molecules in layers further from the surface become progressively more similar to those of bulk liquid water. A quantitative statistical analysis of the MD-generated instantaneous molecular configurations in terms of local density, molecular orientation, nearest neighbor coordination, and the structural details of the H-bonding network shows that the local structure of interfacial water at the brucite surface results from a combination of “hard wall” (geometric and confinement) effects, highly directional H-bonding, and thermal motion. This structure does not resemble that of bulk water at ambient conditions or at elevated or reduced temperature, but shares some similarities with that of water under higher pressure.  相似文献   

15.
Summary High resolution electron micrographs have been obtained from crystals of two types of tourmaline, aligned in a goniometer stage so that the electron beam is parallel to thec axis. Images having a resolution of about 3 Å taken out of focus show direct indications of the atomic arrangement; they suggest medium-range ordering of the metal atoms in buergerite and unexpectedh31l symmetry in elbaite-schorl solid solution. The appearance of ordering is tentatively explained in terms of electron-irradiation effects.
Hochauflösende Elektronenmikroskopie von Turmalinkristallen
Zusammenfassung Hochauflösende Elektronen-Mikrographien wurden von zwei Typen von Turmalinkristallen, die auf einer Goniometereinrichtung so orientiert waren, daß der Elektronenstrahl parallel zurc-Achse verlief, erhalten. Bilder mit einer 3 Å-Auflösung, die entfokusiert aufgenommen wurden, geben direkte Hinweise auf die Atomanordnung; sie deuten auf Ordnung mittlerer Reichweite der Metallatome in Buergerit und zeigen unerwarteterweiseh31l-Symmetrie bei Elbait-Schörl-Mischkristallen. Das Auftreten von Ordnung wird als vermutlicher Elektronenbestrahlungseffekt gedeutet.

With 3 Figures  相似文献   

16.
Bismuth vanadate (microprobe test) in varying shades of orange color and in well developed crystals (averaging 0.2 mm in size) occurs in bismutite in the Mutala granite pegmatite area, district of Zambezia, Mozambique. Two modifications of BiVO 4were identified. An orthorhombic form is identical with pucherite and shows a0 = 5.336 Å, b0 = 5.053 Å, c 0 = 12.021 Å. The crystal habit ranges from platy to stout prismatic. The X-ray powder pattern of the monoclinic form matches that of the synthetic monoclinic Bi-orthovanadate with a 0 = 5.205 Å, b 0 = 11.718 Å, c 0 = 5.098 Å, = 90° 25. The crystal habit resembles that of a pyramidal scheelite crystal with the b-axis corresponding to the scheelite c-axis. Multiple twinning is seen on (101), in some instances with a composition plane (010).  相似文献   

17.
In this paper an analytical method has been proposed to predict the net ultimate uplift capacity of the single bent pile and pile group with a bent embedded in sand considering arching effects. Arching develops due to relative compressibility of sand relative to pile which activates the soil-pile friction. The method takes into consideration the embedded length (L), diameter of the pile (d), bent angle, surface characteristics of pile, group configuration, spacing of the pile group and the soil properties. Log spiral failure surface with parabolic arch shape was assumed in the analysis. Theoretical investigation for uplift capacity was been carried out for the single bent pile and group of pile (2 × 1, 2 × 2) embedded in sand. The variable used in the analysis were embedded length to pile diameter (L/d = 15, 20 and 25), spacing in the group (3d, 4d and 6d) and angle of bent (6°, 14° and 20°). Typical charts for evaluation of net ultimate uplift capacity for pile groups are presented through the figures. Comparison of theoretical results shows good agreement with established experimental results.  相似文献   

18.
In order to investigate directly the structure and properties of grain boundaries in silicate materials undergoing pressure solution, in situ measurements of these properties are required. We report electrical impedance spectroscopy measurements, performed, under hydrothermal conditions, on individual glass–glass and glass-quartz contacts undergoing pressure solution. Resulting estimates of the average grain boundary diffusivity product ( Z = Dd\textav C* Z = D\delta_{\text{av}} C^{*} ) for silica transport and of the average grain boundary fluid film thickness ( d\textav \delta_{\text{av}} ) fall in the ranges 6.3 ± 1.4 × 10−18 m3 s−1 and 350 ± 210 nm, respectively. However, the average values for Z and d\textav \delta_{\text{av}} obtained were likely influenced by cracking and irregular dissolution of the dissolving contact surfaces, rather than representing uniformly wetted grain boundary properties. Post-mortem SEM observations indicate that the contact surfaces were internally rough. Taken together, our data support the notion that during pressure solution of quartz, grain boundary diffusion is rapid, and interface processes (dissolution and precipitation) are more likely to be rate-limiting than diffusion.  相似文献   

19.
Single-crystal X-ray and neutron structure refinements carried out on neptunite (KNa2Li(Fe, Mg, Mn)2Ti2Si8O24) from San Benito, California at various temperatures (neutrons: 15 K and 293 K; X-rays: 110 K, 293 K and 493 K) indicate that this mineral crystallizes in the acentric space group Cc (T=293K: a=16.427 Å, b=12.478 Å, c=9.975 Å, = 115.56°, Z=4, V=1844.53 Å3) due to ordering of octahedrally coordinated metals (Ti, Fe, Mn, Mg). In the neptunite structure, Ti and (Fe, Mn, Mg) octahedra share edges to form chains that run along [110] and [110]. These chains are, in turn, linked through shared corners along [001]. The resulting octahedral framework is interwoven by a similar [Si8O22] tetrahedral framework. Li, Na and K occupy 6-, 8- and 10- coordinated sites within the framework. The metal-containing polyhedra show strong distortions at all temperatures. In particular, Ti exhibits a strong off-center displacement (0.25 Å) within its octahedron, leading to four Ti-O distances of 2.0 Å, one of 2.2 Å and one of 1.7 Å. The displaced Ti position is in good agreement with a position that minimizes differences between ionic bond strengths and is interpreted as an energy minimum in an ionic potential model. Mössbauer spectra collected at 77 K, 293 K and 400 K indicate all Fe to be present as octahedral Fe2+. Although two distinct Fe positions were found in the structure, 77 K and 293 K spectra display only one quadrupole doublet. Two Fe sites can only be resolved in the 400 K spectrum. It is suggested that the temperature dependence of octahedral edge distortions is responsible for the separation of the Mössbauer doublets.  相似文献   

20.
苏皖坡缕石粘土中蛋白石特征及其成因意义   总被引：1，自引：0，他引：1  
TEM和XRD研究表明，在苏皖坡缕石粘土矿床的蛋白石坡缕石层中存在0pal-A和0pal-CT两种结构的蛋白石。蛋白石坡缕石层主要含坡缕石、opal-A、opal-CT，以及少量白云石和其它矿物，由富opal-A层和富opal-CT层互层组成，交互层的厚度在几个厘米左右。蛋白石坡缕石层中的矿物基本是自生矿物，从蒸发湖水中化学沉淀形成。矿物组成特征研究表明，蛋白石坡缕石层的矿物组分(Si、Mg、Al)来源于盆地周围玄武岩淋滤的浅层地下水。根据Opal-A和Opal-CT溶解度图解和城缕石、白云石形成物理化学条件图解，当湖水具有高浓度溶解SiO2和Mg^2 时，有利于opal-A和坡缕石形成，当湖水具有低浓度溶解SiO2时，有利于opal-CT结晶。因此，沉淀SiO2的结构状态取决于地下水补给的湖水溶解SiO2浓度。富opal-A和富opal-CT交互层的形成是古气候、古水文周期性变化的指示。富opal-CT层指示高地下水补给流入量，低蒸发量，湖水低盐度和溶解组分，代表湿润气候时期；而富opal-A层代表低地下水补给流入量，高蒸发量，高溶解组分浓度，代表干旱气候时期。  相似文献   

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